NM_016203.4(PRKAG2):c.1555A>G (p.Thr519Ala) AND Lethal congenital glycogen storage disease of heart

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 2, 2021
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000461963.6

Allele description [Variation Report for NM_016203.4(PRKAG2):c.1555A>G (p.Thr519Ala)]

NM_016203.4(PRKAG2):c.1555A>G (p.Thr519Ala)

Gene:

PRKAG2:protein kinase AMP-activated non-catalytic subunit gamma 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q36.1

Genomic location:

Preferred name:

NM_016203.4(PRKAG2):c.1555A>G (p.Thr519Ala)

HGVS:

NC_000007.14:g.151564107T>C
NG_007486.2:g.318125A>G
NM_001040633.2:c.1423A>G
NM_001304527.2:c.1180A>G
NM_001304531.2:c.832A>G
NM_001363698.2:c.1183A>G
NM_016203.4:c.1555A>GMANE SELECT
NM_024429.2:c.832A>G
NP_001035723.1:p.Thr475Ala
NP_001291456.1:p.Thr394Ala
NP_001291460.1:p.Thr278Ala
NP_001350627.1:p.Thr395Ala
NP_057287.2:p.Thr519Ala
NP_077747.1:p.Thr278Ala
LRG_430t1:c.1555A>G
LRG_430:g.318125A>G
LRG_430p1:p.Thr519Ala
NC_000007.13:g.151261193T>C
NG_007486.1:g.318124A>G
NM_016203.3:c.1555A>G

Protein change:

T278A

Links:

dbSNP: rs1060503024

NCBI 1000 Genomes Browser:

rs1060503024

Molecular consequence:

NM_001040633.2:c.1423A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001304527.2:c.1180A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001304531.2:c.832A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001363698.2:c.1183A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_016203.4:c.1555A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_024429.2:c.832A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Lethal congenital glycogen storage disease of heart
Synonyms:: GLYCOGEN STORAGE DISEASE OF HEART; PHOSPHORYLASE KINASE DEFICIENCY OF HEART
Identifiers:: MONDO: MONDO:0009867; MedGen: C1849813; Orphanet: 439854; OMIM: 261740

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000551575	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Sep 2, 2021)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000551575

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Sep 2, 2021)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000551575.4

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

This sequence change replaces threonine with alanine at codon 519 of the PRKAG2 protein (p.Thr519Ala). The threonine residue is highly conserved and there is a small physicochemical difference between threonine and alanine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with PRKAG2-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C15"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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